Manufacturing Jobs in Hainaut

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QA Associate

Janssen Pharmaceutica

La Louvière

QA on the floor * Act as back-up for EDN QA team, for any other batch disposition activities and version management * QA related experience within an operational pharmaceutical environment. Janssen Pharmaceutica * La Louvière * Contract duration unspecified * Full Time - Your tasks - Operational activities and Quality System Management * Write, review and/or approve Work Instructions (WI) and Procedures (SOP) * Collaborate with other departments for documentation content and ensure - Good Documentation Practices are followed. * Act as delegate of the Responsible Person for the review and approval of activities listed in DS-FRM-36468 (Responsible Person activities delegation list). * Initiate, investigate and/or approve Quality Issues, Correctives and Preventives actions and complaints related to distribution activities and repackaging activities. QA on the floor * Act as back-up for EDN QA team, for any other batch disposition activities and version management * QA related experience within an operational pharmaceutical environment. Janssen Pharmaceutica * La Louvière * Contract duration unspecified * Full Time - Your tasks - Operational activities and Quality System Management * Write, review and/or approve Work Instructions (WI) and Procedures (SOP) * Collaborate with other departments for documentation content and ensure - Good Documentation Practices are followed. * Act as delegate of the Responsible Person for the review and approval of activities listed in DS-FRM-36468 (Responsible Person activities delegation list). * Initiate, investigate and/or approve Quality Issues, Correctives and Preventives actions and complaints related to distribution activities and repackaging activities.
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Inside sales

COSUCRA Groupe Warcoing Sa

Warcoing

In order to support its growth, Cosucra is looking for a: Inside Sales Cosucra is based in Pecq (Warcoing - between Courtrai and Tournai), and offers solutions for a healthy diet through a specialist sales network in more than 45 countries worldwide. • Complete a dynamic team of 4 colleagues in the sales department. • Thoroughly analyze the sales, forecasting and projects to get distributors/customers to achieve their goals. • Feed the Customer Relation Management system (CRM) with sales data. • You have a first experience in Sales Administration (ADM), preferably in the export. COSUCRA Groupe Warcoing Sa * Warcoing * Contract duration unspecified * Full Time - COSUCRA Group Warcoing, ( ), is a Belgian family business incorporated in 1852, producing health ingredients for the global food industry (Inulin – extracted from chicory – along with vegetable proteins, fibres and starch – extracted from yellow peas). Your tasks In order to support its growth, Cosucra is looking for a: Inside Sales Cosucra is based in Pecq (Warcoing - between Courtrai and Tournai), and offers solutions for a healthy diet through a specialist sales network in more than 45 countries worldwide. • Complete a dynamic team of 4 colleagues in the sales department. • Thoroughly analyze the sales, forecasting and projects to get distributors/customers to achieve their goals. • Feed the Customer Relation Management system (CRM) with sales data. • You have a first experience in Sales Administration (ADM), preferably in the export. COSUCRA Groupe Warcoing Sa * Warcoing * Contract duration unspecified * Full Time - COSUCRA Group Warcoing, ( ), is a Belgian family business incorporated in 1852, producing health ingredients for the global food industry (Inulin – extracted from chicory – along with vegetable proteins, fibres and starch – extracted from yellow peas). Your tasks
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QA Validation Specialist

EUMEDICA S.A.

Hainaut

In this role as QA Validation specialist you will define validation strategies in accordance with regulatory requirements and ensure compliance of validation activities at Eumedica site. As QA Validation Specialist, you . • Ensure QA oversight in validation activities (IQ/OQ/PQ...), through CCs, and ensure timely escalation to management of critical issues during validation • Participate in the implementation of the quality systems at Eumedica to ensure compliance and assurance for all validation activities on site like equipment, systems, IT, facilities, utilities • Define the validation strategies in accordance with the regulatory requirements for Eumedica projects and clinical customer projects • Define the validation strategies in accordance with the regulatory requirements • Review/Approve the validation documentation regarding the GMP requirements (knowledge of GMP, Eudralex, GAMP, CFR… In this role as QA Validation specialist you will define validation strategies in accordance with regulatory requirements and ensure compliance of validation activities at Eumedica site. As QA Validation Specialist, you . • Ensure QA oversight in validation activities (IQ/OQ/PQ...), through CCs, and ensure timely escalation to management of critical issues during validation • Participate in the implementation of the quality systems at Eumedica to ensure compliance and assurance for all validation activities on site like equipment, systems, IT, facilities, utilities • Define the validation strategies in accordance with the regulatory requirements for Eumedica projects and clinical customer projects • Define the validation strategies in accordance with the regulatory requirements • Review/Approve the validation documentation regarding the GMP requirements (knowledge of GMP, Eudralex, GAMP, CFR…
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Commercial Assistant (Inside)

TKG

Sint-Genesius-Rode

Assistant (Inside) * Sint-Genesius-Rode * Contract duration unspecified * Full Time - Introduction - A midsized company in the business of small electric household appliances with international contacts and branch offices abroad. The responsibilities - A polyvalent function as department including * administrative tasks (such as invoicing, handling of supplier and customer orders, organization and follow-up of deliveries, …) The profile * diploma: minimum A2 (secundary) * experience of min 1 year in an administrative function * A very good command of English and French * A good command of Dutch * Good knowledge of OFFICE (EXCEL, POWERPOINT, WORD, EXCEL) Your skills * well organized * able to set priorities * respecting deadlines * good communicator * customer-focused * proactive * professional * team player - We offer * A full-time job (40/week with 1 day RTT/month) * A dynamic environment * A positive working atmosphere * Attractive offices in a nice setting Assistant (Inside) * Sint-Genesius-Rode * Contract duration unspecified * Full Time - Introduction - A midsized company in the business of small electric household appliances with international contacts and branch offices abroad. The responsibilities - A polyvalent function as department including * administrative tasks (such as invoicing, handling of supplier and customer orders, organization and follow-up of deliveries, …) The profile * diploma: minimum A2 (secundary) * experience of min 1 year in an administrative function * A very good command of English and French * A good command of Dutch * Good knowledge of OFFICE (EXCEL, POWERPOINT, WORD, EXCEL) Your skills * well organized * able to set priorities * respecting deadlines * good communicator * customer-focused * proactive * professional * team player - We offer * A full-time job (40/week with 1 day RTT/month) * A dynamic environment * A positive working atmosphere * Attractive offices in a nice setting
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QC Analyst

Experis

Hainaut

to QC lab person (Lessines) Review draft Method of Analysis for completeness and feasibility implementation in QC lab. Facilitate the coordination of the validation/transfer activities between R&D and QC laboratory. Collaborate with R&D Analytical SME's, QC Lab Personnel and Analytical Leads to ensure project schedules are met. Good interpersonal skills, and ability to adapt to diverse environments (R&D and QC environment). Experis * Hainaut * Contract duration unspecified * Full Time - Your tasks - Mission description - Ensure training/hands-on on newly developed Analytical Methods as per need and quality processes in place (local and/or general) o From R&D SME - Participate to transfer/validation of analytical method according to study protocol. to QC lab person (Lessines) Review draft Method of Analysis for completeness and feasibility implementation in QC lab. Facilitate the coordination of the validation/transfer activities between R&D and QC laboratory. Collaborate with R&D Analytical SME's, QC Lab Personnel and Analytical Leads to ensure project schedules are met. Good interpersonal skills, and ability to adapt to diverse environments (R&D and QC environment). Experis * Hainaut * Contract duration unspecified * Full Time - Your tasks - Mission description - Ensure training/hands-on on newly developed Analytical Methods as per need and quality processes in place (local and/or general) o From R&D SME - Participate to transfer/validation of analytical method according to study protocol.
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Computerized Systems & Equipment Validation Expert - Pharmaceutical sector

EUMEDICA S.A.

Hainaut

The Validation Expert manages and leads the qualification and validation of Computerized Systems, IT Infrastructure and Equipment. Computerized Systems & Equipment Validation Expert • attend project meetings as Validation Expert The Validation Expert will work within an IT team of 3 people and closely with the CFO. He provides compliance leadership and directions to IT department, business stakeholders and project teams with regards to Computerized Systems Validation (CSV) and IT Infrastructure Qualification. • develop validation / qualification / migration strategies for the Computerized Systems and IT infrastructure per company procedure(s) • manage day to day qualification / validation / periodic review activities / CAPA for the company IT Infrastructure, Computerized Systems and Equipment The Validation Expert manages and leads the qualification and validation of Computerized Systems, IT Infrastructure and Equipment. Computerized Systems & Equipment Validation Expert • attend project meetings as Validation Expert The Validation Expert will work within an IT team of 3 people and closely with the CFO. He provides compliance leadership and directions to IT department, business stakeholders and project teams with regards to Computerized Systems Validation (CSV) and IT Infrastructure Qualification. • develop validation / qualification / migration strategies for the Computerized Systems and IT infrastructure per company procedure(s) • manage day to day qualification / validation / periodic review activities / CAPA for the company IT Infrastructure, Computerized Systems and Equipment
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Project Manager

Institut National des Radio Elements

Fleurus

For the Engineering & Projects department, IRE is looking for a Project Manager (M/F). As Project Manager, you will be dealing with different projects in a radiopharmaceutical environment. * You participate in the conceptual design and the detailed design phases of the projects * You organize and coordinate the necessary resources up to the end of the project, ensure execution as per committed deadlines, scope, budget and required quality; * You analyze and manage project risks; * You lead and coordinate the project team; * You are the main internal/external contact point for the project execution; * You ensure transfer to the process owner and organize project closure; * Industrial or civil engineer in chemistry, biotechnology or electromechanics, you have 10 years of experience preferably in the nuclear industry, the pharmaceutical or chemical sector, including 5 years in project management; For the Engineering & Projects department, IRE is looking for a Project Manager (M/F). As Project Manager, you will be dealing with different projects in a radiopharmaceutical environment. * You participate in the conceptual design and the detailed design phases of the projects * You organize and coordinate the necessary resources up to the end of the project, ensure execution as per committed deadlines, scope, budget and required quality; * You analyze and manage project risks; * You lead and coordinate the project team; * You are the main internal/external contact point for the project execution; * You ensure transfer to the process owner and organize project closure; * Industrial or civil engineer in chemistry, biotechnology or electromechanics, you have 10 years of experience preferably in the nuclear industry, the pharmaceutical or chemical sector, including 5 years in project management;
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